Compositions and methods for mycotoxin decontamination, nucleotide, protein and vitamin enrichment and palatability enhancement of food and animal feed using micronized yeast biomass
a technology of micronized yeast and biomass, which is applied in the field of compositions and methods for mycotoxin decontamination, nucleotide, protein and vitamin enrichment and palatability enhancement of food and animal feed using micronized yeast biomass, can solve the problems of complex quality control protocols necessary to evaluate this property, the inability to distinguish the immunomodulatory benefits of the product, and the high cost of the separation process
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example 1
[0030]To compare the effectiveness of the micronized yeast biomass as a mycotoxin binder versus existing commercial products, an in-vitro mycotoxin binding assay was established. Conditions include adsorption of four mycotoxins typical for North American and European markets—deoxynivalenol (=DON, vomitoxin), ochratoxin (OTA), T-2 toxin and zearalenone (ZEN)—from an aqueous solution, pH 6.5 (0.1 M Na-phosphate buffer), at 37° C. within an hour by 0.5% suspension of the adsorbent candidate. Concentration of each mycotoxin in the mix has been chosen at 1 mg / l (in sum −4.0 mg / l).
[0031]Mycotoxin content in the model aqueous solution was measured using HPLC / MS / MS on a C-8 column eluted by a gradient of formiate buffer->acetonitrile. Under these HPLC conditions mycotoxins are eluted in the following sequence: DON-OTA-T-2-ZEN
example 2
[0032]The biomass of Saccharomyces cerevisiae was produced by submerged fermentation on wheat bran under standard industrial conditions and dried. The dried material was micronized to 5 microns using an orbital mill. The material was tested in-vitro for its mycotoxin binding properties in comparison to the commercial mycotoxin binder Mycosorb (Alltech, Ky.), based on esterified yeast beta-glucan, and yeast / bacterial biomass-based binder Mycofix Plus (Biomin, Austria) using the protocol described in Example 1. The effectiveness of binding four mycotoxins is presented in Table 1.
TABLE 1In-vitro effectiveness of adsorption of four mycotoxins by twocommercial binders and three variants of micronized yeast biomass,alone and in combination with acid hydrolysis lignin.% of mycotoxin adsorbed from aAdsorbent candidate, 5 g / l,mixture of 4 toxins, 1 mg / l eachpH 6.5, 37° C., 1 hourDONOTAT-2ZEACommercial mycotoxin bindersMycosorb (Alltech, Ireland)55.316.16.162.7Mycofix Plus (Biomin, Austria)4....
example 3
[0033]The biomass of Saccharomyces cerevisiae was produced by submerged fermentation on wet distiller's grain under standard industrial conditions and dried. The dried material was milled to 10-30 microns using an impeller mill with the following specifications:
Number of rotors1Position of rotorshorizontalRotation frequency4,500rpmLinear speed of collision70m / secElectrical power consumption30kWMilling capacity120kg / hourMaximal start particle size20mmMaximal hardness of start material, Mohs scale3
[0034]The material was tested for its mycotoxin binding properties in comparison to the commercial yeast esterified beta-glucan based binder Mycosorb (Alltech, Kentucky) and yeast / bacterial biomass based binder Mycofix Plus (Biomin, Austria) in-vitro using the protocol described in Example 1. The effectiveness of initial binding is presented in Table 1.
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